• Ensuring the production proper to the national and international standards, regulations, legislations and guides, 
• Providing fast, practical, efficient and permanent solutions proper to the national and international standards, regulations and legislations for ISO 13485 Quality Management System and 2017/745/EU Medical Device Regulation CE Marking/Certification processes and for issues and obstacles concerning the issues of maintaining the continuousness of these documents after these processes,
• Orientation of the evolving/ changing standards, regulations or legislations and being there for medical device producers all along,
• Ensuring that our producers will be ready not only for inspections done by approved facilities but also for announced or unannounced field inspections done by the T.R. Ministry of Health or for market supervisions.